BEUDAMED
    23 results · 23ms · Sources: EU EUDAMED, US FDA

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    Halyard Pink Underguard Zero, Sterile Powder-Free Exam Gloves Tested with Chemotherapy Drugs

    FDA 510(k)
    FDA Class 1 ·General Hospital

    MEDI

    FDA UDI
    MEDI MANUFACTURING, INC.·04049772777600·LUMBAMED BASIC DORSAL STAY WM SILVER III

    Castanares Facelift Scissors

    FDA UDI
    SONTEC INSTRUMENTS, INC.·00192896113589·Castanares Facelift Scissors Tungsten Carbide/P...

    Endo Carry-On Procedure Kit

    FDA UDI
    MEDIVATORS INC.·00677964080852·Endo Carry-On Procedure Kit

    Endo Carry-On Procedure Kit

    FDA UDI
    MEDIVATORS INC.·00677964102936·Endo Carry-on Procedure Kit includes Suction Tu...

    Endo Carry-On Procedure Kit

    FDA UDI
    MEDIVATORS INC.·00677964101687·Endo Carry-On Procedure Kit

    Endo Carry-On Procedure Kit

    FDA UDI
    MEDIVATORS INC.·00677964083266·Endo Carry-On Procedure Kit

    Endo Carry-On Procedure Kit

    FDA UDI
    MEDIVATORS INC.·00677964101717·Endo Carry-On Procedure Kit

    MODIFICATION TO JMS APHERESIS NEEDLE

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    ABREU, MODEL 700

    FDA 510(k)
    FDA Class 2 ·General Hospital

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·July 29, 2025

    INFUSOR

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - IRVINE·Product code MEB·October 24, 2014

    HOMECHOICE AUTOMATED PD SET WITH CASSETTE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code FKX·August 11, 2011

    INSERT-HANDLE F/ETN RADIOLUC SHORT

    FDA Adverse Event
    Malfunction ·SYNTHES GMBH·Product code FZX·July 2, 2013

    MEDTRONIC TRANSCATHETER VALVE

    FDA Adverse Event
    Injury ·MEDTRONIC HEART VALVES DIVISION·Product code NPT·September 1, 2023

    UNKN ENT REFLEX ULTRA PLASMA WAND AND TURBINATOR WAND

    FDA Adverse Event
    Injury ·ARTHROCARE CORP.·Product code GEI·April 4, 2022

    ROCHE 9180 ELECTROLYTE ANALYZER

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code JFP·September 9, 2025

    IMPLANTABLE NEUROSTIMULATOR

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code LNQ·March 12, 2019

    PROLENE POLYPROPYLENE MESH UNKNOWN PRODUCT

    FDA Adverse Event
    Death ·ETHICON INC.·Product code FTL·September 28, 2018

    PROLENE POLYPROPYLENE MESH UNKNOWN PRODUCT

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code FTL·September 28, 2018